Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Feingold syndrome type 2
Autosomal dominant
Antenatal, Neonatal
Felty syndrome
Unknown
Adult
Female infertility due to oocyte meiotic arrest
Autosomal recessive
Adolescent, Adult
Female infertility due to zona pellucida defect
Autosomal dominant, Autosomal recessive
Adult
Femoral-facial syndrome
Not applicable
Antenatal, Neonatal
Femur-fibula-ulna complex
Not applicable
Antenatal, Neonatal
Ferro-cerebro-cutaneous syndrome
X-linked recessive
Infancy
Ferroportin disease
Fetal Gaucher disease
Autosomal recessive
Infancy, Neonatal
Fetal akinesia deformation sequence
Autosomal recessive
Antenatal, Neonatal
Fetal akinesia-cerebral and retinal hemorrhage syndrome
Autosomal recessive
Infancy, Neonatal
Fetal alcohol syndrome
Not applicable
Antenatal, Neonatal
Fetal and neonatal alloimmune thrombocytopenia
Not applicable
Antenatal, Neonatal
Fetal carbamazepine syndrome
Not applicable
Antenatal, Infancy, Neonatal
Fetal cytomegalovirus syndrome
Not applicable
Antenatal, Neonatal
Fetal encasement syndrome
Autosomal recessive
Antenatal
Fetal hydantoin syndrome
Not applicable
Antenatal, Neonatal
Fetal iodine syndrome
Not applicable
Antenatal, Neonatal
Fetal lung interstitial tumor
Infancy, Neonatal
Fetal methylmercury syndrome
Not applicable
Antenatal, Neonatal
Fetal minoxidil syndrome
Not applicable
Antenatal, Neonatal
Fetal parvovirus syndrome
Not applicable
Antenatal, Neonatal
Fetal trimethadione syndrome
Not applicable
Antenatal, Neonatal
Fetal valproate spectrum disorder
Not applicable
Antenatal, Childhood, Infancy, Neonatal